Molecular basis of the adult i phenotype and the gene responsible for the expression of the human blood group I antigen.
about
Congenital disorder of glycosylation type Id: clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteinsMutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3)A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataractAbnormalities caused by carbohydrate alterations in Ibeta6-N-acetylglucosaminyltransferase-deficient mice.Cat-Map: putting cataract on the mapA novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigreeMolecular characterization of mouse lens epithelial cell lines and their suitability to study RNA granules and cataract associated genesPhase I trial of a novel human monoclonal antibody mAb216 in patients with relapsed or refractory B-cell acute lymphoblastic leukemiaCase report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataractDeletion at the GCNT2 Locus Causes Autosomal Recessive Congenital CataractsCongenital cataracts and their molecular geneticsEpidemiology, clinical manifestations, pathogenesis and laboratory detection of Mycoplasma pneumoniae infections.Pleiotropic effect of a novel mutation in GCNT2 causing congenital cataract and a rare adult i blood group phenotype.Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.An age-dependent ABO discrepancy between mother and baby reveals a novel A(weak) allele.Developmental differences between neonatal and adult human erythropoiesis.A novel IGnT allele responsible for the adult i phenotype.Blood group terminology 2004: from the International Society of Blood Transfusion committee on terminology for red cell surface antigens.Identification of human glycosyltransferase genes expressed in erythroid cells predicts potential carbohydrate blood group loci.Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract.
P2860
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P2860
Molecular basis of the adult i phenotype and the gene responsible for the expression of the human blood group I antigen.
description
2001 nî lūn-bûn
@nan
2001 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Molecular basis of the adult i ...... e human blood group I antigen.
@ast
Molecular basis of the adult i ...... e human blood group I antigen.
@en
Molecular basis of the adult i ...... e human blood group I antigen.
@nl
type
label
Molecular basis of the adult i ...... e human blood group I antigen.
@ast
Molecular basis of the adult i ...... e human blood group I antigen.
@en
Molecular basis of the adult i ...... e human blood group I antigen.
@nl
prefLabel
Molecular basis of the adult i ...... e human blood group I antigen.
@ast
Molecular basis of the adult i ...... e human blood group I antigen.
@en
Molecular basis of the adult i ...... e human blood group I antigen.
@nl
P2093
P1433
P1476
Molecular basis of the adult i ...... e human blood group I antigen.
@en
P2093
P304
P356
10.1182/BLOOD.V98.13.3840
P407
P577
2001-12-01T00:00:00Z